Label: PURELL ADVANCED HAND SANITIZER NOURISHING- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 10, 2018

If you are a consumer or patient please visit this version.

  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help decrease bacteria on skin

  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.  

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    · Put enough product in your palm to thoroughly cover your hands · Rub hands together briskly until dry · Children under 6 years of age should be supervised when using this product

  • Other Information

    • Store below 110°F (43°C) • May discolor certain fabrics or surfaces

  • Inactive Ingredients

    Water (Aqua), Isopropyl Alcohol, Glycerin, Caprylyl Glycol, Isopropyl Myristate, Linum Usitatissimum (Linseed) Seed Extract, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED HAND SANITIZER NOURISHING 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-485
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-485-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product12/30/2016
    2NDC:21749-485-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product12/30/2016
    3NDC:21749-485-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product12/30/2016
    4NDC:21749-485-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product12/30/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/30/2016
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-485)